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4-(2-Ethylphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide
The title compound, C(17)H(16)N(4)OS, is stabilized in the form of a two-dimensional polymeric network due to intermolecular N—H⋯S and N—H⋯O hydrogen bonds. An intramolecular N—H⋯N hydrogen bond forms an S(5) ring, whereas interactions of the N—H⋯O and C—H⋯S types complete S(6) ring motifs. π–π i...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006908/ https://www.ncbi.nlm.nih.gov/pubmed/21587842 http://dx.doi.org/10.1107/S1600536810021264 |
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author | Pervez, Humayun Yaqub, Muhammad Ramzan, Muhammad Tahir, M. Nawaz Iqbal, Mohammad S. |
author_facet | Pervez, Humayun Yaqub, Muhammad Ramzan, Muhammad Tahir, M. Nawaz Iqbal, Mohammad S. |
author_sort | Pervez, Humayun |
collection | PubMed |
description | The title compound, C(17)H(16)N(4)OS, is stabilized in the form of a two-dimensional polymeric network due to intermolecular N—H⋯S and N—H⋯O hydrogen bonds. An intramolecular N—H⋯N hydrogen bond forms an S(5) ring, whereas interactions of the N—H⋯O and C—H⋯S types complete S(6) ring motifs. π–π interactions with a centroid–centroid distance of 3.6514 (10) Å are found between the ethyl-substituted benzene ring and the heterocyclic ring of the isatin derivative. |
format | Text |
id | pubmed-3006908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30069082010-12-30 4-(2-Ethylphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide Pervez, Humayun Yaqub, Muhammad Ramzan, Muhammad Tahir, M. Nawaz Iqbal, Mohammad S. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(17)H(16)N(4)OS, is stabilized in the form of a two-dimensional polymeric network due to intermolecular N—H⋯S and N—H⋯O hydrogen bonds. An intramolecular N—H⋯N hydrogen bond forms an S(5) ring, whereas interactions of the N—H⋯O and C—H⋯S types complete S(6) ring motifs. π–π interactions with a centroid–centroid distance of 3.6514 (10) Å are found between the ethyl-substituted benzene ring and the heterocyclic ring of the isatin derivative. International Union of Crystallography 2010-06-09 /pmc/articles/PMC3006908/ /pubmed/21587842 http://dx.doi.org/10.1107/S1600536810021264 Text en © Pervez et al. 2010 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Pervez, Humayun Yaqub, Muhammad Ramzan, Muhammad Tahir, M. Nawaz Iqbal, Mohammad S. 4-(2-Ethylphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title | 4-(2-Ethylphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title_full | 4-(2-Ethylphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title_fullStr | 4-(2-Ethylphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title_full_unstemmed | 4-(2-Ethylphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title_short | 4-(2-Ethylphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title_sort | 4-(2-ethylphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006908/ https://www.ncbi.nlm.nih.gov/pubmed/21587842 http://dx.doi.org/10.1107/S1600536810021264 |
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